Powell J R, Rogers J F, Wargin W A, Cross R E, Eshelman F N
Arch Intern Med. 1984 Mar;144(3):484-6.
This study was designed to compare the effects of equivalent therapeutic doses of two H2 antagonists, cimetidine and ranitidine, on theophylline pharmacokinetics and to determine whether the previously described cimetidine-theophylline interaction is dose dependent. Twelve healthy adult men were given a 6-mg/kg intravenous aminophylline dose on four occasions. Subjects were randomly assigned four treatments: no treatment (control); cimetidine, 1,200 mg/day; cimetidine, 2,400 mg/day; and ranitidine, 300 mg/day. Cimetidine, 1,200 mg/day, significantly decreased theophylline clearance by 36% (range, 22% to 49%) and increased the mean elimination half-life from 5.7 hours (control) to 9.2 hours. A significant difference was not found between the two cimetidine dosages, indicating dose independence of the interaction over the dosage range studied. Ranitidine did not significantly alter theophylline pharmacokinetics. Theophylline plasma protein binding was not affected by any treatment. The relative effects of cimetidine and ranitidine on the elimination of cytochrome P-450 metabolized drugs such as theophylline indicate a useful property of ranitidine as compared with cimetidine.
本研究旨在比较两种H2拮抗剂西咪替丁和雷尼替丁等效治疗剂量对茶碱药代动力学的影响,并确定先前描述的西咪替丁 - 茶碱相互作用是否存在剂量依赖性。12名健康成年男性分四次静脉注射6 mg/kg氨茶碱剂量。受试者被随机分配接受四种治疗:不治疗(对照);西咪替丁,1200 mg/天;西咪替丁,2400 mg/天;雷尼替丁,300 mg/天。1200 mg/天的西咪替丁显著降低茶碱清除率36%(范围为22%至49%),并使平均消除半衰期从5.7小时(对照)增加到9.2小时。两种西咪替丁剂量之间未发现显著差异,表明在所研究的剂量范围内相互作用不存在剂量依赖性。雷尼替丁未显著改变茶碱药代动力学。任何治疗均未影响茶碱的血浆蛋白结合。西咪替丁和雷尼替丁对细胞色素P-450代谢药物如茶碱消除的相对影响表明,与西咪替丁相比,雷尼替丁具有有益特性。